FDA applicant

L.P. Systems Corp.

Walker, MI2 decisions1982–19950 recalls

FDA records 2 decisions for L.P. Systems Corp. (Walker, MI) from 1982 to 1995: 2 510(k) clearances. All are in product code KCW (Epilator, High Frequency, Needle-Type). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided L.P. Systems Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for L.P. Systems Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — L.P. Systems Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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L.P. Systems Corp.

Which product codes does it file in?

What has FDA decided for it lately?